Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele

Blood Cancer J. 2016 Feb 5;6(2):e392. doi: 10.1038/bcj.2015.81.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alleles*
  • Blood Platelet Disorders / complications*
  • Blood Platelet Disorders / diagnosis
  • Blood Platelet Disorders / genetics*
  • Cell Transformation, Neoplastic / genetics*
  • Core Binding Factor Alpha 2 Subunit / genetics*
  • Female
  • Genetic Association Studies
  • Genetic Predisposition to Disease*
  • Haploinsufficiency*
  • Humans
  • Leukemia, Myeloid, Acute / diagnosis
  • Leukemia, Myeloid, Acute / etiology*
  • Male
  • Middle Aged
  • Pedigree

Substances

  • Core Binding Factor Alpha 2 Subunit